@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_head
{
this:
np:hasAssertion
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_assertion
;
np:hasProvenance
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_provenance
;
np:hasPublicationInfo
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_assertion
a
np:Assertion
.
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_provenance
a
np:Provenance
.
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_assertion
{
miriam-gene:560
a
ncit:C16612
.
lld:C0432474
a
ncit:C7057
.
dgn-gda:DGN58e5535f7878540ffffbe7dcf46cfa9e
sio:SIO_000628
miriam-gene:560
,
lld:C0432474
;
a
sio:SIO_001121
.
}
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_provenance
{
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_assertion
dcterms:description
"[Because of conflicting results about the association between azoospermic patients with Klinefelter syndrome (KFS) and azoospermia factor (AZF) polymorphism, and because nothing is known about the association of KFS with partial AZFc deletions, an association study was performed in Tunisian KFS patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19909597
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP794253.RA3nfl3aHm8Yo7NKu7dNTwdfNF6RNlRAnuxEJcmrBIKSg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}